KCNT1 epilepsy with migrating focal seizures shows a temporal sequence with poor outcome, high mortality and SUDEP
Epilepsy of infancy with migrating focal seizures was first described in 1995. Fifteen years later, KCNT1 gene mutations were identified as the major disease-causing gene of this disease. Currently, the data on epilepsy of infancy with migrating focal seizures associated with KCNT1 mutations are het...
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Artigo |
Idioma: | inglés |
Publicado: |
2019
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Acceso en liña: | https://doi.org/10.1093/brain/awz240 https://academic.oup.com/brain/article-pdf/142/10/2996/30070619/awz240.pdf |
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